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16353-15-4

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16353-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16353-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,5 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16353-15:
(7*1)+(6*6)+(5*3)+(4*5)+(3*3)+(2*1)+(1*5)=94
94 % 10 = 4
So 16353-15-4 is a valid CAS Registry Number.

16353-15-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methyl-4-oxoquinazolin-3-yl)acetohydrazide

1.2 Other means of identification

Product number -
Other names (2-methyl-4-oxo-4H-quinazolin-3-yl)-acetic acid hydrazide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16353-15-4 SDS

16353-15-4Relevant articles and documents

Heterocyclic synthesis: A convenient route to some 2-mercepto 1,3,4-oxadiazole and green chemistry microwave-induced one-pot synthesis of 2-aryl 1,3,4-oxadiazole in quinazolone and their antibacterial and antifungal activity

Desai,Desai

, p. 995 - 999 (2007/10/03)

Several 6-substituted-3-[(5-mercepto-1,3,4-oxadiazol-2-yl)methyl]-2- substituted quinazolin-4(3H)-one or 6-substituted-3-[4-(5-mercepto-1,3,4- oxadiazol-2-yl)phenyl]-2-substituedquinazolin-4(3H)-one 2(a-l) and 6-substituted-3-[(5-phenyl-1,3,4-oxadiazol-2-yl)methyl]-2-substitutedquinazolin- 4(3H)-one or 6-substituted-3-[4-(5-phenyl-1,3,4-oxadiazol-2-yl) phenyl]-2-substitutedquinazolin-4(3H)-one 3(a-l) were synthesized using conventional and microwave techniques respectively and were screened for antibacterial and antifungal activity.

Synthesis and Biological Activity of 3-(5-Aryl-1,3,4-oxadiazol-2-ylmethyl)-2-methyl-4(3H)-quinazolinones

Rao, A. Devender,Shankar, Ch. Ravi,Rao, A. Bhaskar,Reddy, V. Malla

, p. 665 - 667 (2007/10/02)

Fourteen 3-(5-aryl-1,3,4-oxadiazol-2-ylmethyl)-2-methyl-4(3H)-quinazolinones (IV) have been prepared by condensation of the respective 2-methyl-4-oxo-3-quinazolineacetic acid hydrazides with different aromatic carboxylic acids in the presence of phosphoro

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